familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
MONDO:0014747Mondo
Findings
No curated finding names familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
- Inheritance
- Autosomal dominant inheritance
HPO, annotations 2026-09-02
Features
5 features
What the disease is reported to present with, and how often among people who have it — never how often a feature means the disease. HPO, annotations 2026-09-02.
- Iris colobomaHPOHP:0000612
- 6 of 9 reported patients · Congenital onset
- Developmental cataractHPOHP:0000519
- Posterior synechiae of the anterior chamberHPOHP:0011484
- Reduced visual acuityHPOHP:0007663
- Retinal atrophyHPOHP:0001105
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- HGNC:31582HGNC:31582
- Strong · Labcorp Genetics (formerly Invitae) · Autosomal dominant · 2020
- Moderate · PanelApp Australia · Autosomal dominant · 2025
- Limited · Ambry Genetics · Autosomal dominant · 2024
- Limited · G2P · Autosomal dominant · 2017
Where it sits
Other names
1 name
Resolves to: familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome
- Also called
- retinal dystrophy and iris coloboma with or without cataract